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Sengupta, T. K.

Publications and source records attributed to Sengupta, T. K..

2 recordsLinked to original sources

Effect of Lantana camara ethanolic leaf extract on survival and migration of MDA-MB-231 triple negative breast cancer cell line

IntroductionBreast cancer is a leading cause of cancer-related death worldwide. Lantana camara has been reported to cure a number of ailments, with few studies showing its cytotoxic effects on breast cancer cells. However, the impact of Lantana camara on triple negative breast cancer cells is largely obscure to date. The present study investigated the effect of ethanolic extract of Lantana camara leaves on the triple negative breast cancer cell line, MDA-MB-231. MethodsCytotoxic effect of the extract on the cells was determined by cell survival assay. Cell cycle phase distribution was analysed using flow cytometry. To study the effect on nuclear morphology, nuclear stained cells were visualized using epifluorescence microscopy. The induction of apoptosis and generation of reactive oxygen species was conducted using flow cytometry. Cellular migration was studied by performing wound healing assay. Real-time polymerase chain reaction was done to determine the mRNA levels of some key genes. ResultsLantana camara leaf extract induced cytomorphological changes and growth inhibitory effect on MDA-MB-231 cells in a dose-dependent manner. The extract also induced G0/G1 cell cycle arrest and nuclear condensation. Flow cytometry analysis confirmed cell death by apoptosis. Lantana camara leaf extract also reduced the migration of MDA-MB-231 cells. mRNA expression levels also supported the above observations. ConclusionsThis study demonstrates the efficacy of the extract to induce growth-inhibitory and anti-migratory effects on MDA-MB-231 cells. Our results thus suggest that Lantana camara leaf extract can be considered as a potent source of chemotherapeutic agents for triple negative breast cancer.

cancer biology↗

Antibiotic induced biofilm formations in Pseudomonas aeruginosa strains KPW.1-S1 and HRW.1-S3 are associated with increased production of eDNA and exoproteins, increased ROS generation, and increased cell surface hydrophobicity

Pseudomonas aeruginosa is a medically important bacteria due to its ability to form biofilm and is also an opportunistic pathogen. Pseudomonas aeruginosa has the intrinsic ability to form biofilm as one of the defense mechanisms for their survival. The fact that it can form biofilms on various medical implants makes it more harmful clinically. Although various antibiotics are used to treat Pseudomonas aeruginosa infections, previous studies have shown that sub-MIC levels of antibiotics cause biofilm formation in this type of bacteria. The present study thus deals with the effect of the aminoglycoside antibiotic gentamicin on the biofilm dynamics of two Pseudomonas aeruginosa strains KPW.1-S1 and HRW.1-S3. Biofilm formation was seen to be increasing with increased gentamicin concentrations in growth media. Confocal laser scanning microscopy and scanning electron microscopy accompanied with other biochemical tests deduced that biofilm-forming components like exoproteins, eDNA, and exolipids as exopolymeric substances in Pseudomonas aeruginosa biofilms were increased in the presence of gentamicin. An increase in reactive oxygen species generation along with increased cell surface hydrophobicity was also seen in both strains when treated with gentamicin. The observed increase in the adherence of the cells accompanied by an increase in exopolymeric substances, eDNA, and exolipids may have largely contributed to the increased biofilm production by the Pseudomonas aeruginosa strains KPW.1-S1 and HRW.1-S3 under the stress of the antibiotic treatment.

microbiology↗